IL216609A0 - Preparation and uses of 1,2,4-triazolo [1,5a] pyridine derivatives - Google Patents
Preparation and uses of 1,2,4-triazolo [1,5a] pyridine derivativesInfo
- Publication number
- IL216609A0 IL216609A0 IL216609A IL21660911A IL216609A0 IL 216609 A0 IL216609 A0 IL 216609A0 IL 216609 A IL216609 A IL 216609A IL 21660911 A IL21660911 A IL 21660911A IL 216609 A0 IL216609 A0 IL 216609A0
- Authority
- IL
- Israel
- Prior art keywords
- triazolo
- preparation
- pyridine derivatives
- pyridine
- derivatives
- Prior art date
Links
- DACWQSNZECJJGG-UHFFFAOYSA-N [1,2,4]triazolo[1,5-a]pyridine Chemical class C1=CC=CN2N=CN=C21 DACWQSNZECJJGG-UHFFFAOYSA-N 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D455/00—Heterocyclic compounds containing quinolizine ring systems, e.g. emetine alkaloids, protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine
- C07D455/02—Heterocyclic compounds containing quinolizine ring systems, e.g. emetine alkaloids, protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine containing not further condensed quinolizine ring systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US18453309P | 2009-06-05 | 2009-06-05 | |
| PCT/US2010/037363 WO2010141796A2 (fr) | 2009-06-05 | 2010-06-04 | Préparation et utilisation de dérivés de 1,2,4-triazolo[1,5a]pyridine |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IL216609A0 true IL216609A0 (en) | 2012-02-29 |
Family
ID=42985748
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL216609A IL216609A0 (en) | 2009-06-05 | 2011-11-24 | Preparation and uses of 1,2,4-triazolo [1,5a] pyridine derivatives |
Country Status (14)
| Country | Link |
|---|---|
| US (2) | US8501936B2 (fr) |
| EP (1) | EP2438066A2 (fr) |
| JP (1) | JP5684245B2 (fr) |
| KR (1) | KR20120044966A (fr) |
| CN (1) | CN102459258B (fr) |
| AU (1) | AU2010254806C1 (fr) |
| BR (1) | BRPI1009637A2 (fr) |
| CA (1) | CA2763900A1 (fr) |
| CL (1) | CL2011003082A1 (fr) |
| IL (1) | IL216609A0 (fr) |
| MX (1) | MX2011012961A (fr) |
| NZ (1) | NZ597140A (fr) |
| TW (1) | TWI500614B (fr) |
| WO (1) | WO2010141796A2 (fr) |
Families Citing this family (47)
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|---|---|---|---|---|
| WO2009155565A1 (fr) * | 2008-06-20 | 2009-12-23 | Genentech, Inc. | Composés triazolopyridine inhibiteurs de jak kinase et procédés |
| CN102131389A (zh) | 2008-06-20 | 2011-07-20 | 健泰科生物技术公司 | 三唑并吡啶jak抑制剂化合物和方法 |
| JO3041B1 (ar) | 2008-07-25 | 2016-09-05 | Galapagos Nv | مركبات جديدة مفيدة لمعالجة الأمراض التنكسية والالتهابية |
| JO3030B1 (ar) | 2009-06-26 | 2016-09-05 | Galapagos Nv | مركب جديد مفيد لمعالجة الامراض التنكسية والالتهابات |
| TWI462920B (zh) | 2009-06-26 | 2014-12-01 | 葛萊伯格有限公司 | 用於治療退化性及發炎疾病之新穎化合物 |
| EP2343294A1 (fr) | 2009-11-30 | 2011-07-13 | Bayer Schering Pharma AG | Triazolopyridines substituées |
| EA201300282A1 (ru) * | 2010-08-27 | 2013-08-30 | Мерк Патент Гмбх | Производные триазолопиразина |
| CA2818936A1 (fr) | 2010-12-06 | 2012-06-14 | Cephalon, Inc. | Traitement d'inflammation chronique avec un derive de 1,2,4-triazolo[1,5a]pyridine |
| EP2648728B1 (fr) * | 2010-12-06 | 2016-04-27 | Cephalon, Inc. | Inhibiteur de la janus kinase 2 (jak2) pour le traitement du lupus |
| US20130324532A1 (en) | 2011-02-17 | 2013-12-05 | Cancer Therapeutics Crc Pty Limited | Fak inhibitors |
| US9174946B2 (en) | 2011-02-17 | 2015-11-03 | Cancer Therapeutics Crc Pty Ltd | Selective FAK inhibitors |
| TWI577693B (zh) * | 2011-05-31 | 2017-04-11 | 江蘇康緣藥業股份有限公司 | 聚(adp-核糖)聚合酶之三環抑制劑 |
| ES3018133T3 (en) | 2011-11-30 | 2025-05-14 | Univ Emory | Jak inhibitors for use in the prevention or treatment of a viral disease caused by a coronaviridae |
| KR20130091464A (ko) | 2012-02-08 | 2013-08-19 | 한미약품 주식회사 | 타이로신 카이네이즈 억제 활성을 갖는 트리아졸로피리딘 유도체 |
| CN104114557B (zh) * | 2012-02-21 | 2017-10-24 | 默克专利股份公司 | 作为syk酪氨酸激酶抑制剂和gcn2丝氨酸激酶抑制剂的8‑取代2‑氨基‑[1,2,4]三唑并[1,5‑a]吡嗪 |
| US20150051202A1 (en) * | 2012-03-07 | 2015-02-19 | Merck Patent Gmbh | Triazolopyrazine derivatives |
| US9284311B2 (en) * | 2012-06-22 | 2016-03-15 | Galapagos Nv | Aminotriazolopyridine for use in the treatment of inflammation, and pharmaceutical compositions thereof |
| SG11201408419QA (en) * | 2012-07-10 | 2015-01-29 | Bayer Pharma AG | Method for preparing substituted triazolopyridines |
| SG11201500261VA (en) * | 2012-07-27 | 2015-02-27 | Novartis Ag | Prediction of treatment response to jak/stat inhibitor |
| US20160123982A1 (en) | 2013-02-04 | 2016-05-05 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for assaying jak2 activity in red blood cells and uses thereof |
| PE20161323A1 (es) * | 2013-09-05 | 2016-11-25 | Hoffmann La Roche | Compuestos de triazolopiridina, composiciones y metodos de uso de los mismos |
| GB201402070D0 (en) | 2014-02-07 | 2014-03-26 | Galapagos Nv | Pharmaceutical compositions for the treatment of inflammatory disorders |
| GB201402071D0 (en) | 2014-02-07 | 2014-03-26 | Galapagos Nv | Novel salts and pharmaceutical compositions thereof for the treatment of inflammatory disorders |
| JP2018507236A (ja) * | 2015-03-04 | 2018-03-15 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | トリアゾロピリジン化合物及びその使用法 |
| KR102598246B1 (ko) * | 2016-07-26 | 2023-11-02 | 톈진 롱보진 파마시우티컬 씨오., 엘티디. | Jak 저해제로서 헤테로사이클릭 화합물, 및 이의 염 및 치료학적 용도 |
| CN107759587B (zh) * | 2016-08-19 | 2021-01-26 | 中国医药研究开发中心有限公司 | [1,2,4]三唑并[1,5-a]吡啶类化合物及其制备方法和医药用途 |
| CN109890817B (zh) * | 2016-09-06 | 2022-06-17 | 豪夫迈·罗氏有限公司 | 8-(氮杂环丁烷-1-基)-[1,2,4]三唑并[1,5-a]吡啶基化合物、其组合物和应用方法 |
| CN107880038B (zh) * | 2016-09-30 | 2021-09-28 | 中国医药研究开发中心有限公司 | [1,2,4]三唑并[1,5-a]吡啶类化合物及其制备方法和医药用途 |
| EA039352B1 (ru) * | 2017-01-19 | 2022-01-17 | Сучжоу Лонгбайотек Фармасьютикалз Ко., Лтд. | Соединение в качестве селективного ингибитора jak и его соли и терапевтическое применение |
| WO2018167283A1 (fr) | 2017-03-17 | 2018-09-20 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Procédés pour le diagnostic et le traitement d'un remodelage neuronal associé à un adénocarcinome canalaire pancréatique |
| EP3610264A1 (fr) | 2017-04-13 | 2020-02-19 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Procédés de diagnostic et de traitement d'un adénocarcinome canalaire pancréatique |
| WO2020092015A1 (fr) | 2018-11-02 | 2020-05-07 | University Of Rochester | Atténuation thérapeutique d'une infection épithéliale |
| JP2022509019A (ja) | 2018-11-05 | 2022-01-20 | シンジェンタ パーティシペーションズ アーゲー | 殺有害生物的に活性なアゾール-アミド化合物 |
| US12522583B2 (en) | 2018-11-07 | 2026-01-13 | Dana-Farber Cancer Institute, Inc. | Benzimidazole derivatives and aza-benzimidazole derivatives as Janus kinase 2 inhibitors and uses thereof |
| EP3877371A4 (fr) | 2018-11-07 | 2022-07-27 | Dana-Farber Cancer Institute, Inc. | Dérivés d'imidazopyridine et dérivés d'aza-imidazopyridine utilisés comme inhibiteurs de la janus kinase 2 et utilisations associées |
| EP3876939A4 (fr) | 2018-11-07 | 2022-08-10 | Dana-Farber Cancer Institute, Inc. | Dérivés benzothiazoles et dérivés 7-aza benzothiazoles comme inhibiteurs de la janus kinase 2 et leurs utilisations |
| AU2019395201A1 (en) | 2018-12-06 | 2021-05-20 | Daiichi Sankyo Company, Limited | Cycloalkane-1,3-diamine derivative |
| CA3137152A1 (fr) | 2019-04-18 | 2020-10-22 | The Johns Hopkins University | Derives de 2-amino-pyrazolyl-[1,2,4]triazolo[1,5a] pyridine substitues et leur utilisation |
| CN111057059B (zh) * | 2019-11-25 | 2022-04-26 | 广东省测试分析研究所(中国广州分析测试中心) | 一种苯并二四氢吡咯类化合物或其药学上可接受的盐、及其制备方法和应用 |
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| AU2021362678A1 (en) | 2020-10-13 | 2023-05-04 | The Johns Hopkins University | SUBSTITUTED 4-([1,2,4]TRIAZOLO[1,5-a]PYRIDIN-6-YL)THIOPHENE-2-CARBOXAMIDE DERIVATIVES AND USE THEREOF |
| US12043632B2 (en) | 2020-12-23 | 2024-07-23 | Ajax Therapeutics, Inc. | 6-heteroaryloxy benzimidazoles and azabenzimidazoles as JAK2 inhibitors |
| WO2023009708A1 (fr) * | 2021-07-29 | 2023-02-02 | Ajax Therapeutics, Inc. | Hétéroaryloxy triazolo-azines et imidazo-azines en tant qu'inhibiteurs de jak2 |
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| JO3041B1 (ar) | 2008-07-25 | 2016-09-05 | Galapagos Nv | مركبات جديدة مفيدة لمعالجة الأمراض التنكسية والالتهابية |
| WO2010010184A1 (fr) | 2008-07-25 | 2010-01-28 | Galapagos Nv | [1, 2, 4]triazolo[1, 5-a]pyridines utilisées comme inhibiteurs de jak |
| WO2010010186A1 (fr) | 2008-07-25 | 2010-01-28 | Galapagos Nv | Nouveaux composés utiles pour le traitement de maladies dégénératives et inflammatoires |
| WO2010010188A1 (fr) | 2008-07-25 | 2010-01-28 | Galapagos Nv | Nouveaux composés utiles pour le traitement de maladies dégénératives et inflammatoires |
| WO2010010189A1 (fr) | 2008-07-25 | 2010-01-28 | Galapagos Nv | Nouveaux composés utiles pour le traitement de maladies dégénératives et inflammatoires |
| WO2010010187A1 (fr) | 2008-07-25 | 2010-01-28 | Galapagos Nv | Nouveaux composés utiles pour le traitement de maladies dégénératives et inflammatoires |
| US20100041891A1 (en) * | 2008-08-12 | 2010-02-18 | Takeda Pharmaceutical Company Limited | Amide compound |
| TWI453207B (zh) | 2008-09-08 | 2014-09-21 | Signal Pharm Llc | 胺基三唑并吡啶,其組合物及使用其之治療方法 |
| JP2010070503A (ja) | 2008-09-19 | 2010-04-02 | Daiichi Sankyo Co Ltd | 抗真菌作用2−アミノトリアゾロピリジン誘導体 |
| WO2010057877A1 (fr) | 2008-11-18 | 2010-05-27 | Cellzome Limited | Triazolo[1,5-a]pyridines 7-pyridinyle- ou phényl-substituées comme inhibiteurs de pi3k |
| HRP20160488T1 (hr) | 2008-12-19 | 2016-06-17 | Leo Pharma A/S | Triazolopiridini kao inhibitori fosfodiesteraze za liječenje kožnih bolesti |
| WO2010092015A1 (fr) | 2009-02-10 | 2010-08-19 | Cellzome Limited | Dérivés d'urée-triazolo[1,5-a]pyridine en tant qu'inhibiteurs de pi3k |
| SG173610A1 (en) | 2009-02-13 | 2011-09-29 | Fovea Pharmaceuticals Sa | [1, 2, 4] triazolo [1, 5 -a] pyridines as kinase inhibitors |
| EP2523949B1 (fr) * | 2010-01-15 | 2014-08-20 | Janssen Pharmaceuticals Inc. | Nouveaux dérivés de triazole en tant que modulateurs de la secrétase gamma |
-
2010
- 2010-06-04 EP EP10724213A patent/EP2438066A2/fr not_active Withdrawn
- 2010-06-04 WO PCT/US2010/037363 patent/WO2010141796A2/fr not_active Ceased
- 2010-06-04 CA CA2763900A patent/CA2763900A1/fr not_active Abandoned
- 2010-06-04 BR BRPI1009637-0A patent/BRPI1009637A2/pt not_active IP Right Cessation
- 2010-06-04 KR KR1020127000197A patent/KR20120044966A/ko not_active Abandoned
- 2010-06-04 JP JP2012514166A patent/JP5684245B2/ja not_active Expired - Fee Related
- 2010-06-04 US US12/793,984 patent/US8501936B2/en active Active
- 2010-06-04 AU AU2010254806A patent/AU2010254806C1/en not_active Ceased
- 2010-06-04 NZ NZ597140A patent/NZ597140A/en unknown
- 2010-06-04 CN CN201080024761.0A patent/CN102459258B/zh not_active Expired - Fee Related
- 2010-06-04 TW TW099118109A patent/TWI500614B/zh not_active IP Right Cessation
- 2010-06-04 MX MX2011012961A patent/MX2011012961A/es active IP Right Grant
-
2011
- 2011-11-24 IL IL216609A patent/IL216609A0/en unknown
- 2011-12-05 CL CL2011003082A patent/CL2011003082A1/es unknown
-
2013
- 2013-06-18 US US13/920,153 patent/US8633173B2/en active Active
Also Published As
| Publication number | Publication date |
|---|---|
| US8501936B2 (en) | 2013-08-06 |
| CA2763900A1 (fr) | 2010-12-09 |
| TW201100421A (en) | 2011-01-01 |
| AU2010254806C1 (en) | 2016-07-07 |
| TWI500614B (zh) | 2015-09-21 |
| NZ597140A (en) | 2014-01-31 |
| AU2010254806B2 (en) | 2016-02-04 |
| US8633173B2 (en) | 2014-01-21 |
| KR20120044966A (ko) | 2012-05-08 |
| CL2011003082A1 (es) | 2012-06-08 |
| AU2010254806A1 (en) | 2012-01-19 |
| US20130296312A1 (en) | 2013-11-07 |
| CN102459258B (zh) | 2015-11-25 |
| JP5684245B2 (ja) | 2015-03-11 |
| CN102459258A (zh) | 2012-05-16 |
| US20100311693A1 (en) | 2010-12-09 |
| BRPI1009637A2 (pt) | 2019-04-30 |
| WO2010141796A3 (fr) | 2012-02-16 |
| EP2438066A2 (fr) | 2012-04-11 |
| JP2012528886A (ja) | 2012-11-15 |
| MX2011012961A (es) | 2012-01-30 |
| WO2010141796A2 (fr) | 2010-12-09 |
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